Autism, susceptibility to, 20

Preferred Label : Autism, susceptibility to, 20;

Symbol : AUTS20;

CISMeF acronym : AUTS20;

Type : Phenotype, molecular basis known;

Inheritance : Autosomal dominant;

Molecular basis : Susceptibility conferred by mutation in the neuroligin-1 gene (NLGN1, 600568.0001);

Prefixed ID : #618830;

Details

Origin ID

618830;

UMLS CUI

C5394226;

Genes related to phenotype
- Neuroligin 1 [OMIM gene]
HPO term(s)
- Attention deficit hyperactivity disorder [HPO term]
- Autistic behavior [HPO term]
- Autosomal dominant inheritance [HPO term]
- Global developmental delay [HPO term]
- Impaired social interactions [HPO term]
- Obsessive-compulsive behavior [HPO term]
Semantic type(s)
- Finding [UMLS semantic type]

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